Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Raimos M. Olomi"'
Publikováno v:
Case Reports in Genetics, Vol 2012 (2012)
Cornelia de Lange syndrome is a dominantly inherited, genetically heterogeneous and clinically variable syndrome with multiple congenital anomalies and developmental delay. Gastrointestinal anomalies are common and an important cause of morbidity and
Externí odkaz:
https://doaj.org/article/34515edbfdf244aa9b0763516d791907
Publikováno v:
Case Reports in Genetics, Vol 2012 (2012)
Case Reports in Genetics
Case Reports in Genetics
Cornelia de Lange syndrome is a dominantly inherited, genetically heterogeneous and clinically variable syndrome with multiple congenital anomalies and developmental delay. Gastrointestinal anomalies are common and an important cause of morbidity and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d427e5f6d2ac3ed1a8f53c24e82a79e9
https://doaj.org/article/34515edbfdf244aa9b0763516d791907
https://doaj.org/article/34515edbfdf244aa9b0763516d791907